GB1138374A - Process for the preparation of polystyrene with a great impact resistance - Google Patents

Process for the preparation of polystyrene with a great impact resistance

Info

Publication number
GB1138374A
GB1138374A GB4806066A GB4806066A GB1138374A GB 1138374 A GB1138374 A GB 1138374A GB 4806066 A GB4806066 A GB 4806066A GB 4806066 A GB4806066 A GB 4806066A GB 1138374 A GB1138374 A GB 1138374A
Authority
GB
United Kingdom
Prior art keywords
styrene
vinyl
acid
acids
ester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB4806066A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of GB1138374A publication Critical patent/GB1138374A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

1,138,374. Impact - resistant polystyrene. SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ N.V. 26 Oct., 1966 [28 Oct., 1965], No. 48060/66. Heading C3G. An impact-resistant polymer is produced by polymerizing a solution of at least one synthetic rubber and/or natural rubber in at least one styrene (as hereinafter defined), the polymerization being performed in the presence of at least one styrene-soluble carbonyloxy compound containing more than 8 carbon atoms and at least one olefinic double bond and which can be represented by the formula in which R 1 is hydrogen or a substituted or unsubstituted hydrocarbon radical and R 2 is a hydrocarbon radical, or has been obtained by reaction of an epoxy resin with an olefinically unsaturated carboxylic acid. The term " styrene includes alkyl styrenes, alphamethyl styrene, divinyl benzene and vinyl naphthalenes. The carbonyloxy compound is for instance an alkyl or alkenyl ester of an unsaturated carboxylic acid, e.g. oleic, linoleic, linolenic or 10-undecylenic acid, or an alkenyl ester of a saturated carboxylic acid, e.g. vinyl and 1-methyl vinyl esters of stearic, palmitic, myristic, lauric and caproic acids or of acids with quaternary or tertiary α-carbon atoms. Compounds other than the rubber and carbonyloxy compound may be dissolved in the styrene, e.g. a monomer such as acrylonitrile, acrylic acid, methacrylic acid, an ester of such an acid or a diene, or other macromolecular substances. In the examples, polybutadiene is dissolved in styrene along with a compound selected from vinyl stearate, a vinyl ester of a mixture of branched C 9- C 11 -carboxylic acids, 2-ethylhexyl acrylate and an epichlorohydrin/diphenylolpropane condensation product esterified with fatty acids of linseed oil. The resulting solutions are polymerized using dilauryl peroxide as catalyst.
GB4806066A 1965-10-28 1966-10-26 Process for the preparation of polystyrene with a great impact resistance Expired GB1138374A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL6513957A NL6513957A (en) 1965-10-28 1965-10-28

Publications (1)

Publication Number Publication Date
GB1138374A true GB1138374A (en) 1969-01-01

Family

ID=19794494

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4806066A Expired GB1138374A (en) 1965-10-28 1966-10-26 Process for the preparation of polystyrene with a great impact resistance

Country Status (4)

Country Link
BE (1) BE688907A (en)
DE (1) DE1645395A1 (en)
GB (1) GB1138374A (en)
NL (1) NL6513957A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116809041A (en) * 2023-08-31 2023-09-29 凯莱英生命科学技术(天津)有限公司 Hydrophilic polystyrene-divinylbenzene porous microsphere, preparation method and application thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116809041A (en) * 2023-08-31 2023-09-29 凯莱英生命科学技术(天津)有限公司 Hydrophilic polystyrene-divinylbenzene porous microsphere, preparation method and application thereof
CN116809041B (en) * 2023-08-31 2023-12-08 凯莱英生命科学技术(天津)有限公司 Hydrophilic polystyrene-divinylbenzene porous microsphere, preparation method and application thereof

Also Published As

Publication number Publication date
DE1645395A1 (en) 1970-07-30
NL6513957A (en) 1967-05-02
BE688907A (en) 1967-04-26

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